專業權威 · 完整履歷 · 即時門診
馬偕紀念醫院
主治醫師
生育保健學科暨遺傳諮詢中心
產前診斷、遺傳諮詢、分子細胞遺傳學、周產期醫學、畸胎學、臨床遺傳學
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馬偕紀念醫院生育保健學科主治醫師
陽明大學護理研究所及醫學院醫學系兼任教授
高雄醫學院醫學系畢業
美國耶魯大學遺傳學系研究員
美國耶魯大學遺傳學系研究醫師
馬偕紀念醫院婦產部優生保健學科主任
台灣婦產科醫學會副理事長、常務理事
馬偕紀念醫院醫學研究部主任
兼任教授: 國立陽明大學、國立交通大學、中國醫藥大學、亞洲大學
馬偕紀念醫院婦產部主任
台灣周產期醫學會理事長
教育部部定教授 (國立陽明大學送審)
馬偕紀念醫院副院長
產前診斷、遺傳諮詢、分子細胞遺傳學、周產期醫學、畸胎學、臨床遺傳學
Chih-Ping Chen. Prenatal diagnosis and genetic counseling of omphalocele: an overview and atlas of cases. Elsevier Taiwan LLC, 2007. ISBN 978-986-83792-0-6.
Chih-Ping Chen. Prenatal diagnosis and genetic counseling of omphalocele: an overview and atlas of cases. Elsevier Taiwan LLC, 2007. ISBN 978-986-83792-0-6.
Chih-Ping Chen. Prenatal diagnosis and genetic counseling of neural tube defects: an overview and atlas of cases. Elsevier Taiwan LLC, 2009. ISBN 978-986-6538-23-0.
Chih-Ping Chen. Prenatal diagnosis and genetic counseling of neural tube defects: an overview and atlas of cases. Elsevier Taiwan LLC, 2009. ISBN 978-986-6538-23-0.
論文研究(2015年):
Chih-Ping Chen, Jun-Wei Su, Schu-Rern Chern, Yu-Ling Kuo, Peih-Shan Wu, Meng-Shan Lee, Chien-Wen Yang, Wayseen Wang. Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis. Taiwan J Obstet Gynecol 2015; 54: 58-61.
Chih-Ping Chen, Jun-Wei Su, Schu-Rern Chern, Yu-Ling Kuo, Peih-Shan Wu, Meng-Shan Lee, Chien-Wen Yang, Wayseen Wang. Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis. Taiwan J Obstet Gynecol 2015; 54: 58-61.
Chih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, Yu-Peng Liu, Cheng-Ran Peng, Yu-Ling Kuo, Peih-Shan Wu, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia. Taiwan J Obstet Gynecol 2015; 54: 66-70.
Chih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, Yu-Peng Liu, Cheng-Ran Peng, Yu-Ling Kuo, Peih-Shan Wu, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia. Taiwan J Obstet Gynecol 2015; 54: 66-70.
Chih-Ping Chen, Tsang-Ming Ko, Ming-Chao Huang, Schu-Rern Chern, Tan-Wei Lin, Tung-Yao Chang, Yu-Ling Kuo, Wen-Lin Chen, Wayseen Wang. Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma. Taiwan J Obstet Gynecol 2015; 54: 78-80.
Chih-Ping Chen, Tsang-Ming Ko, Ming-Chao Huang, Schu-Rern Chern, Tan-Wei Lin, Tung-Yao Chang, Yu-Ling Kuo, Wen-Lin Chen, Wayseen Wang. Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma. Taiwan J Obstet Gynecol 2015; 54: 78-80.
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